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Prader-Willi Syndrome: Clinical Aspects

1 Jan 2012

Abstract excerpt

Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient's life. The syndrome is due to the loss of expression of several genes encoded on the proximal long arm of chromosome 15 (15q11.2-q13). The complex phenotype is most probably caused by a hypothalamic dysfunction that is responsible for hormonal dysfunctions and for...

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PMID: 23133744
DOI: 10.1155/2012/473941

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